3736-31-0

Basic information

• Product Name: 1H-Indole-5,6-dione, 2,3-dihydro-3-hydroxy-1-(1-methylethyl)-
• CAS NO: 3736-31-0
• Molecular Formula: C11H13NO3
• Mol File: 3736-31-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1H-Indole-5,6-dione, 2,3-dihydro-3-hydroxy-1-(1-methylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole-5,6-dione, 2,3-dihydro-3-hydroxy-1-(1-methylethyl)-(3736-31-0)
• EPA Substance Registry System: 1H-Indole-5,6-dione, 2,3-dihydro-3-hydroxy-1-(1-methylethyl)-(3736-31-0)

Safety Data

• Hazardous Substances Data: 3736-31-0(Hazardous Substances Data)

Usage

Physical appearance

Yellowish crystalline compound

Derivative of

Indole

Uses

Synthesis of various pharmaceuticals

Known for

Antiviral, antibacterial, and anticancer properties

Potential as

Neuroprotective agent

Subject of

Numerous studies

Field of interest

Medicinal chemistry

Upstream product

• 7683-59-2 isoproterenol 
• 114-45-4 1-(3,4-dihydroxy-phenyl)-2-isopropylamino-ethanol; sulfate 

Relevant articles and documents

New derivatives of adrenochrome.

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Photoproducts and proposed degradation pathway in the riboflavin-sensitised photooxidation of isoproterenol

Products of the aerobic visible-light-promoted riboflavin-sensitised photooxidation of the sympathomimetic drug isoproterenol were identified by means of HPLC and spectrophotometric techniques. The oxidative process, mediated by superoxide radical anion, generates N-isopropylaminochrome as a main photoproduct with a quantum yield of 0.15. In parallel, the photodecomposition of riboflavin is prevented in the presence of isoproterenol. A reaction scheme for the photooxidation pathway of isoproterenol is proposed in analogy to former reports for related compounds.

Anodische Synthese von N-Isopropylnoradrenochrommonosemicarbazon

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